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Biomedical subjects

W Raab

Publications and source records attributed to W Raab.

At least 37 records · Page 2Linked to original sources

The effects of analgesics on pain-related somatosensory evoked potentials.

Human cerebral evoked potentials can be employed to test the effectiveness of analgesics. In the present study, pain-related cortical responses were elicited by chemical stimulation of the nasal mucosa in combination with electrical stimulation of dental pulp. In alternating sequence, 16 series of 6 chemical and 6 electrical stimuli each were presented. Interstimulus and interseries intervals were 2 s and 50-60 s, respectively. Stimulus intensities were 54% carbon dioxide (v/v) and 4 dB over the electrical current threshold of 21-45 microA for noxious chemical and electrical stimulation, respectively. Four volunteers participated in the study. The EEG was recorded at 8 sites of the international 10-20 system. After each series of stimuli, the test subjects, using visual analogue scales, rated pain intensity relative to a single standard stimulus they had received initially. After running through the procedure once, without their noticing it, the subjects intravenously received 5 ml (2.5 g) metamizol or 5 ml 0.9% NaCl, which were slowly (over a period of 12 min) added to an infusion. The entire stimulation procedure was then repeated 10 min later. Whereas the evoked potentials clearly exhibited habituation effects due to stimulus repetition within a series, the latter were absent in the subjects' pain ratings. Despite the comparatively high i.v. dose of 2.5 g metamizol, pain ratings markedly different from those given under placebo were not observed. In contrast, potential amplitudes after metamizol administration exhibited a clear tendency towards smaller amplitudes in both types of stimulation. In addition, metamizol effects on pain rating could be demonstrated successfully by applying continual chemical stimulation.

Analgesics

[Psoriasis therapy with fumaric acid and fumaric acid esters].

Fumaric acid may not be regarded as an antipsoriatic drug. Beneficial effects on psoriatic lesions may be explained by secondary changes such as the acidification of gastric juice in cases of anacidity or hypacidity . Monoethylfumarate exerts true antipsoriatic activities but is by far too toxic for clinical use. Experimental investigations have confirmed an inhibitory action of the above-mentioned fumarate on nucleic acid synthesis and protein synthesis of PHA-stimulated human lymphocytes.

DNA

[The activity of imidazole derivatives in the presence of human plasma (author's transl)].

By Warburg technique using yeasts and staphylococci, any decrease in antimicrobial activity of the imidazole derivatives could be excluded in the presence of human plasma. Econazole nitrate, the classical topical imidazole derivative, and ketoconazole, an oral active antifungal, were tested. The compatibility between imidazole derivatives and human plasma is of practical importance for obtaining optimal therapeutic results in treating human mycoses.

Antifungal Agents

[Serum hydroxyproline parameter of collagen metabolism (author's transl)].

The serum hydroxyproline level enables a clinical assessment to be made of bone metabolism. A clinical-chemical method, which is described in detail, was applied in 50 control persons as well as in 76 patients with diseases of bones and/or joints. This method, which is a modification of the standard ion-exchange method of Goverde and Veenkamp for the determination of free hydroxyproline in serum, is readily applicable to mass routine laboratory usage and may be repeated ad libitum, thereby facilitating control follow-up of therapeutic response. The mean value of serum free hydroxyproline in the normal control group was 11.9 mu mol/1 (range: 6.86 to 16 mu mol/1), i.e. 1.56 mg/1 (range: 0.9 to 21 mg/1). The upper limit of normal values was calculated to be 15.5 mu mol/1 (2.0 mg/1), allowing a clear-cut differentiation from pathologically raised levels above this value.

Adult

Active absorption of hypoxanthine by lamb jejunum in vitro.

The kinetics of [3H]hypoxanthine entry into lamb mid-jejunum were measured using 2-min mucosal exposures. Mucosal hypoxanthine uptake occurred by a Na+- and energy-dependent saturable mechanism indicating that a carrier-mediated active transport process is involved. Inhibitory measurements indicate that hypoxanthine, adenosine, uracil and thymine complete for a common entry mechanism. Adenine, uric acid, allantoin and thymidine produced no significant inhibition of hypoxanthine entry. In additional experiments hypoxanthine was transported against a high concentration gradient from the mucosal to the serosal side of everted sacs of mid-jejunum. Therefore hypoxanthine appears to be absorbed by active transport from the lamb jejunum.

Animals

Glucose-6-phosphatase dehydrogenase activity in rat urine. Changes following kidney damage (short report).

In rat urine, G-6-PDH activity is regularly present. Following the administration of nephrotoxic substances (D-serine, tetrathionate), or after elicitation of vascular shock (hypoxic kidney damage), a statistically significant increase in urinary G-6-PDH activity occurs. The alterations in urinary G-6-PDH activity largely correspond to the changes in urinary AP activity which, in this study, was determined in all of the experiments.

Alkaline Phosphatase

[Effect of imidazole derivatives on various numbers of microbes to determine microbial sensitivity].

Imidazole derivatives with antifungal activity were investigated in their effects on concentrated and diluted suspensions of Saccharomyces cerevisiae, Candida albicans, and Staphylococcus aureus haemolyticus. Against Candida albicans, activity of the imidazol derivatives was higher in diluted suspensions than in concentrated suspensions: this fact proves the presence of a microbe-count sensitivity. Against Saccharomyces cerevisiae and Staphylococcus aureus haemolyticus, no microbe-count sensitivity of clotrimazole, econazole nitrate, ketoconazole, or N-148/76 could be detected by Warburg assay on resting microbes.

Candida albicans